# K080590: Aos Proximal Humeral Plate

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Orthopaedic Solutions, Inc.
- Decided: May 6, 2008 after 64 days
- Product code: KTW (Appliance, Fixation, Nail/Blade/Plate Combination, Single Component)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K011815 (2001). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011815: Synthes LCP Proximal Humerus Plates, Synthes (Usa) (2001) Summary page 1.

## Cited in the summary but kept off the family tree
- K041806: Passing Needle with Ethibond, Panacryl or Orthocord Suture; and Passing Needle with Ethibond Loop, Depuy Mitek, A Johnson & Johnson Company (2004). Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Most influential descendants
- K160409: AOS Anterolateral Proximal Humeral Plate (2016), 1 descendant of its own
- K171606: AOS Anterolateral Proximal Humeral Plate (2017), 0 descendants of its own

## Indications for use
The AOS Proximal Humeral Plate is indicated for fractures, fracture dislocations, osteotomies, and non-unions of the proximal humerus.

Source page: https://510kreport.com/device/K080590
Methodology: https://510kreport.com/methodology